Evidence map›Paper›PMID 41039368›Full record

ArticleBMC pediatrics2025

The timing of using IVIG for neonatal ABO hemolytic disease.

Na Ma, Feihong Zhang, Yong Hu, Bin Xia

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Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Na MaDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Feihong ZhangDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Yong HuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, China. huyong1003@163.com.
Bin XiaDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, China. xiabin1972@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundABO hemolytic disease of the newborn (ABO HDN) is the most prevalent cause of hemolytic disease of the newborn, often leading to hyperbilirubinemia. In some cases, ABO HDN can progress to significant hyperbilirubinemia. The role of intravenous immunoglobulin (IVIG) in treating ABO HDN remains controversial. Several key questions regarding significant hyperbilirubinemia remain unanswered: What are the risk factors of ABO HDN with significant hyperbilirubinemia? Can IVIG provide benefits for ABO HDN with significant hyperbilirubinemia? Where do we place IVIG in the treatment sequence paradigm of ABO HDN? How do we best stratify ABO HDN with significant hyperbilirubinemia for IVIG therapy?

methodsWe conducted a retrospective cohort study include 948 newborns from West China Second University Hospital, divided into two groups according to the use/nonuse of IVIG. The maternal and neonatal baseline clinical data were collected from digital medical record system. The risk factors of the significant hyperbilirubinemia associated with ABO HDN were investigated using univariate and multivariate analysis. The generalized additive mixed model (GAMM) was used to analyze the nonlinear relationship of bilirubin level with different treatment over time.

resultsA total of 948 newborns fulfilled the inclusion criteria, with 143 (15.1%) in the IVIG group, and 805 (84.9%) in the non-IVIG group. (1) The multivariate analysis found that gestational age ≥ 37 weeks (OR 4.19; p = 0.019), age at admission range 24-48 h (OR 9.69; p = 0.03) and age at admission >48 h (OR 50.31; p < 0.0001) were affect significant hyperbilirubinemia in neonates. (2) The total serum bilirubin (TSB) descent speed of IVIG group (0.69µmol/L/h, 95%CI, 0.48-0.89µmol/L/h) was higher than non-IVIG group (0.21µmol/L/h, 95%CI, 0.14-0.29µmol/L/h) among the neonates with age at admission ≤ 48 h (p < 0.0001);No adverse effects related to IVIG treatment were recorded in either group.

conclusionRegular monitoring of TSB levels starting 24 h after birth is an effective strategy to prevent severe hyperbilirubinemia in ABO HDN. For southwest Chinese neonates, IVIG should not be routinely used to treat ABO HDN in those admitted > 48 h after birth.

Indexed as

ABO Blood-Group SystemErythroblastosis, FetalImmunoglobulins, IntravenousImmunologic FactorsBilirubinFemaleHumansHyperbilirubinemia, NeonatalInfant, NewbornMaleRetrospective StudiesRisk FactorsTime FactorsABO Blood-Group SystemBilirubinImmunoglobulins, IntravenousImmunologic FactorsABO blood groupHemolytic disease of the newbornHyperbilirubinemiaIntravenous immunoglobin (IVIG)Neonatal jaundiceRisk factors

Identifiers

PMID41039368
PMCPMC12492713

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.